کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2058527 1543963 2014 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
In- silico exploration of thirty alphavirus genomes for analysis of the simple sequence repeats
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوشیمی، ژنتیک و زیست شناسی مولکولی (عمومی)
پیش نمایش صفحه اول مقاله
In- silico exploration of thirty alphavirus genomes for analysis of the simple sequence repeats
چکیده انگلیسی


• This is the first analysis of SSR and cSSR in alphaviruses.
• We analysed differential frequency and distribution patterns of SSRs and cSSRs.
• We studied localization of SSR and cSSR in alphaviruses proteomics
• This study would help in better understanding of evolutionary biology of alphaviruses.

The compilation of simple sequence repeats (SSRs) in viruses and its analysis with reference to incidence, distribution and variation would be instrumental in understanding the functional and evolutionary aspects of repeat sequences. Present study encompasses the analysis of SSRs across 30 species of alphaviruses. The full length genome sequences, assessed from NCBI were used for extraction and analysis of repeat sequences using IMEx software. The repeats of different motif sizes (mono- to penta-nucleotide) observed therein exhibited variable incidence across the species. Expectedly, mononucleotide A/T was the most prevalent followed by dinucleotide AG/GA and trinucleotide AAG/GAA in these genomes. The conversion of SSRs to imperfect microsatellite or compound microsatellite (cSSR) is low. cSSR, primarily constituted by variant motifs accounted for up to 12.5% of the SSRs. Interestingly, seven species lacked cSSR in their genomes. However, the SSR and cSSR are predominantly localized to the coding region ORFs for non structural protein and structural proteins. The relative frequencies of different classes of simple and compound microsatellites within and across genomes have been highlighted.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Meta Gene - Volume 2, December 2014, Pages 694–705
نویسندگان
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